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Hereditas|October 7, 1998
Detailed genetic and physical mapping in the Sjögren-Larsson syndrome gene region in 17p11.2A Sillén, A Alderborn, M Pigg, et al.Ophthalmic Genetics|July 13, 2001
Best's vitelliform macular dystrophy caused by a new mutation (Val89Ala) in the VMD2 geneL Eksandh, B Bakall, B Bauer, et al.Acta Paediatrica (Oslo, Norway : 1992)|December 1, 1996
Achondroplasia in Sweden caused by the G1138A mutation in FGFR3A Alderborn, M Anvret, K H Gustavson, et al.Genetic Counseling (Geneva, Switzerland)|January 1, 1996
Hyperkalemic periodic paralysis caused by recurring mutation in the adult muscle sodium channel alpha-subunit geneA Sillén, C Wadelius, M Sundvall, et al.Clinical Genetics|March 1, 1997
Genetic mapping using fluorescent quantification of allele frequencies in pooled DNA loaded by solid supportC Graff, A Persson, P J Ulfendahl, et al.Clinical Genetics|January 1, 1993
Hemophilia B in a 46,XX female probably caused by non-random X inactivationC Wadelius, M Lindstedt, M Pigg, et al.Pharmacogenetics|December 11, 1999
Prostate cancer associated with CYP17 genotypeM Wadelius, A O Andersson, J E Johansson, et al.Human Genetics|January 24, 1998
Refined genetic localization of the Best disease gene in 11q13 and physical mapping of linked markers on radiation hybridsC Graff, A Eriksson, K Forsman, et al.Genetic Counseling (Geneva, Switzerland)|January 23, 1999
Linkage analysis excludes familial congenital hypothyroidism from chromosome 21B E Ahlbom, M Yaqoob, G Annerén, et al.Acta Dermato-Venereologica|March 23, 1999
Further evidence of genetic homogeneity in Sjögren-Larsson syndromeM Pigg, I Annton-Lamprecht, C Braun-Quentin, et al.Pageof 5